229 related articles for article (PubMed ID: 12439895)
21. Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.
Suzuki T; Delgado-Escueta AV; Alonso ME; Morita R; Okamura N; Sugimoto Y; Bai D; Medina MT; Bailey JN; Rasmussen A; Ramos-Peek J; Cordova S; Rubio-Donnadieu F; Ochoa A; Jara-Prado A; Inazawa J; Yamakawa K
Neurosci Lett; 2006 Sep; 405(1-2):126-31. PubMed ID: 16876319
[TBL] [Abstract][Full Text] [Related]
22. Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
Martínez-Juárez IE; Alonso ME; Medina MT; Durón RM; Bailey JN; López-Ruiz M; Ramos-Ramírez R; León L; Pineda G; Castroviejo IP; Silva R; Mija L; Perez-Gosiengfiao K; Machado-Salas J; Delgado-Escueta AV
Brain; 2006 May; 129(Pt 5):1269-80. PubMed ID: 16520331
[TBL] [Abstract][Full Text] [Related]
23. Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.
Marini C; Scheffer IE; Crossland KM; Grinton BE; Phillips FL; McMahon JM; Turner SJ; Dean JT; Kivity S; Mazarib A; Neufeld MY; Korczyn AD; Harkin LA; Dibbens LM; Wallace RH; Mulley JC; Berkovic SF
Epilepsia; 2004 May; 45(5):467-78. PubMed ID: 15101828
[TBL] [Abstract][Full Text] [Related]
24. Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
Berkovic SF; Serratosa JM; Phillips HA; Xiong L; Andermann E; Díaz-Otero F; Gómez-Garre P; Martín M; Fernández-Bullido Y; Andermann F; Lopes-Cendes I; Dubeau F; Desbiens R; Scheffer IE; Wallace RH; Mulley JC; Pandolfo M
Epilepsia; 2004 Sep; 45(9):1054-60. PubMed ID: 15329069
[TBL] [Abstract][Full Text] [Related]
25. A gene for autosomal dominant congenital nystagmus localizes to 6p12.
Kerrison JB; Arnould VJ; Barmada MM; Koenekoop RK; Schmeckpeper BJ; Maumenee IH
Genomics; 1996 May; 33(3):523-6. PubMed ID: 8661013
[TBL] [Abstract][Full Text] [Related]
26. Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity.
Stöber G; Seelow D; Rüschendorf F; Ekici A; Beckmann H; Reis A
Hum Genet; 2002 Oct; 111(4-5):323-30. PubMed ID: 12384773
[TBL] [Abstract][Full Text] [Related]
27. No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.
Durner M; Shinnar S; Resor SR; Moshe SL; Rosenbaum D; Cohen J; Harden C; Kang H; Hertz S; Wallace S; Luciano D; Ballaban-Gil K; Greenberg DA
Am J Med Genet; 2000 Feb; 96(1):49-52. PubMed ID: 10686551
[TBL] [Abstract][Full Text] [Related]
28. Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients.
Durner M; Sander T; Greenberg DA; Johnson K; Beck-Mannagetta G; Janz D
Neurology; 1991 Oct; 41(10):1651-5. PubMed ID: 1922810
[TBL] [Abstract][Full Text] [Related]
29. A novel gene in the chromosomal region for juvenile myoclonic epilepsy on 6p12 encodes a brain-specific lysosomal membrane protein.
Suzuki T; Ganesh S; Agarwala KL; Morita R; Sugimoto Y; Inazawa J; Delgado-Escueta AV; Yamakawa K
Biochem Biophys Res Commun; 2001 Nov; 288(3):626-36. PubMed ID: 11676489
[TBL] [Abstract][Full Text] [Related]
30. Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
Ma S; Blair MA; Abou-Khalil B; Lagrange AH; Gurnett CA; Hedera P
Epilepsy Res; 2006 Oct; 71(2-3):129-34. PubMed ID: 16839746
[TBL] [Abstract][Full Text] [Related]
31. Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.
Elmslie FV; Williamson MP; Rees M; Kerr M; Kjeldsen MJ; Pang KA; Sundqvist A; Friis ML; Richens A; Chadwick D; Whitehouse WP; Gardiner RM
Am J Hum Genet; 1996 Sep; 59(3):653-63. PubMed ID: 8751867
[TBL] [Abstract][Full Text] [Related]
32. Mapping genes in juvenile myoclonic epilepsy.
Delgado-Escueta AV; Greenberg DA
Rev Neurol (Paris); 1987; 143(5):351-62. PubMed ID: 2889252
[TBL] [Abstract][Full Text] [Related]
33. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.
Whitehouse WP; Rees M; Curtis D; Sundqvist A; Parker K; Chung E; Baralle D; Gardiner RM
Am J Hum Genet; 1993 Sep; 53(3):652-62. PubMed ID: 8352275
[TBL] [Abstract][Full Text] [Related]
34. Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.
Hempelmann A; Heils A; Sander T
Epilepsy Res; 2006 Oct; 71(2-3):223-8. PubMed ID: 16876983
[TBL] [Abstract][Full Text] [Related]
35. Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Suzuki T; Delgado-Escueta AV; Aguan K; Alonso ME; Shi J; Hara Y; Nishida M; Numata T; Medina MT; Takeuchi T; Morita R; Bai D; Ganesh S; Sugimoto Y; Inazawa J; Bailey JN; Ochoa A; Jara-Prado A; Rasmussen A; Ramos-Peek J; Cordova S; Rubio-Donnadieu F; Inoue Y; Osawa M; Kaneko S; Oguni H; Mori Y; Yamakawa K
Nat Genet; 2004 Aug; 36(8):842-9. PubMed ID: 15258581
[TBL] [Abstract][Full Text] [Related]
36. Genetic linkage study of an autosomal recessive form of juvenile myoclonic epilepsy in a consanguineous Tunisian family.
Layouni S; Salzmann A; Guipponi M; Mouthon D; Chouchane L; Dogui M; Malafosse A
Epilepsy Res; 2010 Jun; 90(1-2):33-8. PubMed ID: 20378313
[TBL] [Abstract][Full Text] [Related]
37. Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy.
Pal DK; Durner M; Klotz I; Dicker E; Shinnar S; Resor S; Cohen J; Harden C; Moshé SL; Ballaban-Gill K; Bromfield EB; Greenberg DA
Brain Dev; 2006 Mar; 28(2):92-8. PubMed ID: 16414227
[TBL] [Abstract][Full Text] [Related]
38. A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26.
Puranam RS; Jain S; Kleindienst AM; Saxena S; Kim MK; Kelly Changizi B; Padma MV; Andrews I; Elston RC; Tiwari HK; McNamara JO
Ann Neurol; 2005 Sep; 58(3):449-58. PubMed ID: 16130088
[TBL] [Abstract][Full Text] [Related]
39. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA
Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098
[TBL] [Abstract][Full Text] [Related]
40. No evidence of linkage to 6p markers in spanish families with juvenile myoclonic epilepsy.
Obach V; Arroyo S; Santamaria J; Grinberg D; Oliva R
Neurosci Lett; 2000 Jun; 286(3):213-7. PubMed ID: 10832022
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
